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Merck
CN

51261

(-)-儿茶素

puriss., ≥98.5% (HPLC)

别名:

(-)--3,3′,4′5,7-五羟基黄烷, (2S,3R)-2-(3,4-二羟基苯基)-3,4-二氢-1 (2H)-苯并吡喃-3,5,7-三醇

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关于此项目

经验公式(希尔记法):
C15H14O6
化学文摘社编号:
分子量:
290.27
EC Number:
242-611-7
UNSPSC Code:
12352200
MDL number:
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grade

puriss.

assay

≥98.5% (HPLC)

storage temp.

2-8°C

SMILES string

O[C@@H]1Cc2c(O)cc(O)cc2O[C@H]1c3ccc(O)c(O)c3

InChI

1S/C15H14O6/c16-8-4-11(18)9-6-13(20)15(21-14(9)5-8)7-1-2-10(17)12(19)3-7/h1-5,13,15-20H,6H2/t13-,15+/m1/s1

InChI key

PFTAWBLQPZVEMU-HIFRSBDPSA-N



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Woo Duck Seo et al.
Bioorganic & medicinal chemistry letters, 15(24), 5514-5516 (2005-10-06)
Chalcones 1-20, a new class of glycosidase inhibitors, were synthesized, and their glycosidase inhibitory activities were investigated. Non-aminochalcones 1-12 had no inhibitory activity, however, aminochalcones 13-20 had strong glycosidase (alpha-glucosidase, alpha-amylase, and beta-amylase) inhibitory activities. In particular, sulfonamide chalcones 17-20
Christine A Larsen et al.
Journal of medicinal chemistry, 52(21), 6543-6545 (2009-10-21)
Most cancer deaths result from spread of the primary tumor to distant sites (metastasis). MET is an important protein for metastasis in multiple tumor types. Here we report on the ability of tea catechins to suppress MET activation in human
Eui Seok Shin et al.
Bioorganic & medicinal chemistry, 16(7), 3580-3586 (2008-03-04)
Recent studies have shown that glucose-6-phosphate dehydrogenase (G6PD) is an effectual therapeutic target for metabolic disorders, including obesity and diabetes. In this study, we used in silico and conventional screening approaches to identify putative inhibitors of G6PD and found that